Korntner Stefanie H, Jana Aniket, Kinnard Elizabeth, Leo Emily, Beane Timothy, Li Xianmu, Sengupta Rohit, Becker Lauren, Kuo Catherine K
Fischell Department of Bioengineering, University of Maryland, College Park, MD, United States.
Department of Biomedical Engineering, University of Rochester, Rochester, NY, United States.
Front Cell Dev Biol. 2022 Sep 7;10:944126. doi: 10.3389/fcell.2022.944126. eCollection 2022.
Craniofacial (CF) tendons are often affected by traumatic injuries and painful disorders that can severely compromise critical jaw functions, such as mastication and talking. Unfortunately, tendons lack the ability to regenerate, and there are no solutions to restore their native properties or function. An understanding of jaw tendon development could inform tendon regeneration strategies to restore jaw function, however CF tendon development has been relatively unexplored. Using the chick embryo, we identified the jaw-closing Tendon of the musculus Adductor Mandibulae Externus (TmAM) and the jaw-opening Tendon of the musculus Depressor Mandibulae (TmDM) that have similar functions to the masticatory tendons in humans. Using histological and immunohistochemical (IHC) analyses, we characterized the TmAM and TmDM on the basis of cell and extracellular matrix (ECM) morphology and spatiotemporal protein distribution from early to late embryonic development. The TmAM and TmDM were detectable as early as embryonic day (d) 9 based on histological staining and tenascin-C (TNC) protein distribution. Collagen content increased and became more organized, cell density decreased, and cell nuclei elongated over time during development in both the TmAM and TmDM. The TmAM and TmDM exhibited similar spatiotemporal patterns for collagen type III (COL3), but differential spatiotemporal patterns for TNC, lysyl oxidase (LOX), and matrix metalloproteinases (MMPs). Our results demonstrate markers that play a role in limb tendon formation are also present in jaw tendons during embryonic development, implicate COL3, TNC, LOX, MMP2, and MMP9 in jaw tendon development, and suggest TmAM and TmDM possess different developmental programs. Taken together, our study suggests the chick embryo may be used as a model with which to study CF tendon extracellular matrix development, the results of which could ultimately inform therapeutic approaches for CF tendon injuries and disorders.
颅面(CF)肌腱常受创伤性损伤和疼痛性疾病影响,这些会严重损害关键的颌功能,如咀嚼和说话。不幸的是,肌腱缺乏再生能力,且尚无恢复其天然特性或功能的解决办法。了解颌肌腱发育可为恢复颌功能的肌腱再生策略提供信息,然而CF肌腱发育相对未被充分探索。利用鸡胚,我们确定了与人类咀嚼肌腱功能相似的咬肌外侧头肌的闭口肌腱(TmAM)和降颌肌的开口肌腱(TmDM)。通过组织学和免疫组织化学(IHC)分析,我们根据细胞和细胞外基质(ECM)形态以及从胚胎早期到晚期发育的时空蛋白分布对TmAM和TmDM进行了表征。基于组织学染色和肌腱蛋白-C(TNC)蛋白分布,最早在胚胎第9天就能检测到TmAM和TmDM。在TmAM和TmDM的发育过程中,随着时间推移,胶原蛋白含量增加且排列更有序,细胞密度降低,细胞核拉长。TmAM和TmDM在III型胶原蛋白(COL3)方面表现出相似的时空模式,但在TNC、赖氨酰氧化酶(LOX)和基质金属蛋白酶(MMPs)方面表现出不同的时空模式。我们的结果表明,在肢体肌腱形成中起作用的标志物在胚胎发育期间的颌肌腱中也存在,表明COL3、TNC、LOX、MMP2和MMP9参与颌肌腱发育,并提示TmAM和TmDM具有不同的发育程序。综上所述,我们的研究表明鸡胚可作为研究CF肌腱细胞外基质发育的模型,其结果最终可为CF肌腱损伤和疾病的治疗方法提供信息。